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Mean platelet volume, an indicator of platelet reactivity,
is increased in patients with patent foramen ovale
Ercan Varol, Bayram A. Uysal, Ibrahim Ersoy, Mehmet Ozaydin, Dogan Erdogan
and Abdullah Dogan
Numerous studies have shown an association between
patent foramen ovale (PFO) and cryptogenic stroke
suggesting that paradoxical emboli may be an important
cause of stroke. In addition, some authors have proposed
that platelet activation is present in PFO patients and this
might be the cause of the stroke. The aim of this study was
to assess the mean platelet volume (MPV), an indicator of
platelet activation and/or reactivity in patients with PFO. The
study group consisted of 77 patients with PFO. An age, sex,
BMI-matched control group was composed of 43 healthy
volunteers. We measured serum MPV values in patients and
controls. MPV was significantly higher among PFO patients
when compared with control group (9.0 W 0.8 vs. 8.3 W 0.9 fl,
respectively; P < 0.001). We have shown that MPV was
significantly elevated in patients with PFO compared with
controls. Blood Coagul Fibrinolysis 24:605–607 ß 2013
Wolters Kluwer Health | Lippincott Williams & Wilkins.
Blood Coagulation and Fibrinolysis 2013, 24:605–607
Keywords: mean platelet volume, patent foramen ovale, platelet activation,
stroke
Department of Cardiology, Suleyman Demirel University, Isparta, Turkey
Correspondence to Ercan Varol, Department of Cardiology, Suleyman Demirel
Univesitesi Tip Fakultesi, Isparta, Turkey
Tel: +90 246 211 9346; e-mail: drercanvarol@yahoo.com
Received 12 December 2012 Revised 13 February 2013
Accepted 13 February 2013
Introduction
Approximately 25–40% of strokes are of undetermined
pathogenesis, and are commonly termed cryptogenic
strokes. Numerous studies have shown an association
between patent foramen ovale (PFO) and cryptogenic
strokes suggesting that paradoxical emboli (i.e. emboli
crossing from the venous to arterial circulation through a
PFO may be an important cause of cryptogenic strokes
[1–5]. On the contrary, two prospective studies failed
to confirm PFO as an independent risk factor for crypto-
genic strokes, with only an insignificant trend toward a
higher incidence of stroke in persons with PFO [6,7].
Mean platelet volume (MPV) is a simple and easy
method of assessing platelet function [8,9]. In comparison
to smaller ones, larger platelets have more granules,
aggregate more rapidly with collagen, have higher
thromboxane A2 level and express more glycoprotein
Ib and IIb/IIIa receptors [10–12].
It has been accepted that PFO is a potential route for
embolic transit of platelet aggregations, thrombi, gas
bubbles or other particulate matter from the systemic
venous circulation to the brain. PFO also could be a nidus
for potentially embolic thrombus formation in situ [13].
To the best of our knowledge, there is no data assessing
MPV, an indicator of platelet activation and/or reactivity
in patients with PFO. In this study, we evaluated MPV,
an indicator of platelet reactivity, in patients with PFO.
Patients and methods
The study group consisted of 77 patients with PFO
(46 women, 31 men, mean age 34.2 23.0 years)
admitted to our university hospital between 2008
and 2012. An age and sex-matched control group was
composed of 43 healthy volunteers (27 women, 16 men
with a mean age 37.3 12.4 years). The study was
approved by the institutional ethics committee and all
patients gave their informed consent.
Exclusion criteria were moderate to severe mitral and/
or aortic valve disease, coronary artery disease, acute
coronary syndromes, left ventricular systolic dysfunction,
atrial fibrillation, hypertension, diabetes mellitus, dysli-
pidemia, history of renal or liver disease, malignancy,
venous thrombosis, systemic or pulmonary embolism,
congenital hemorrhagic disease, thrombocytopenia,
thrombocytosis, transfusion, acute or chronic inflam-
matory disease, autoimmune disease or current use of
oral contraceptives, anticoagulant or antiplatelet drugs
and statins.
Echocardiography
Both transthoracic and transesophageal echocardio-
graphies (GE VingMed System FiVe, Norway) with
tissue harmonics were performed by two experienced
investigators. M-mode measurements were obtained
from parasternal long-axis view for left atrium diameter,
end-diastolic and end-systolic diameters of the left
ventricle, septum and posterior wall thickness according
to the recommendations of the American Society
of Echocardiography. Left ventricular ejection fraction
was calculated by Simpson’s method. A transesophageal
echocardiography was performed by 7.5-MHz multiplane
transducer at 08 (four-chamber view), 458 (aortic short
Original article 605
0957-5235 ß 2013 Wolters Kluwer Health | Lippincott Williams & Wilkins DOI:10.1097/MBC.0b013e32836029ee